Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells
Niemann T, Joneleit J, Storm J, Nacke T, Wähnert D, Kaltschmidt C, Vordemvenne T, Kaltschmidt B (2023)
Cells 12(23): 2683.
Zeitschriftenaufsatz
| Veröffentlicht | Englisch
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Autor*in
Niemann, Tarek;
Joneleit, Jonas;
Storm, JonathanUniBi;
Nacke, Tom;
Wähnert, DirkUniBi;
Kaltschmidt, ChristianUniBi;
Vordemvenne, ThomasUniBi;
Kaltschmidt, BarbaraUniBi
Einrichtung
Abstract / Bemerkung
Sex-related differences are a current topic in contemporary science. In addition to hormonal regulation, cell-autonomous mechanisms are important in bone homeostasis and regeneration. In this study, human skeletal stem cells (SSCs) from female and male adults were cultured and analyzed with immunological assays and osteogenic differentiation assessments. Female SSCs exhibited a mean doubling time of 100.6 h, whereas male SSCs displayed a mean doubling time of 168.0 h. Immunophenotyping revealed the expression of the stem cell markers Nestin, CD133, and CD164, accompanied by the neural-crest marker SOX9. Furthermore, multiparameter flow cytometric analyses revealed a substantial population of multipotent SSCs, comprising up to 80% in both sexes. An analysis of the osteogenic differentiation potential demonstrated a strong mineralization in both male and female SSCs under physiological conditions. Recognizing the prevailing association of bone diseases with inflammatory processes, we also analyzed the osteogenic potential of SSCs from both sexes under pro-inflammatory conditions. Upon TNF-α and IL-1β treatment, we observed no sexual dimorphism on osteogenesis. In summary, we demonstrated the successful isolation and characterization of SSCs capable of rapid osteogenic differentiation. Taken together, in vitro cultured SSCs might be a suitable model to study sexual dimorphisms and develop drugs for degenerative bone diseases.
Stichworte
skeletal stem cells;
sex dimorphism;
osteogenic differentiation;
inflammation;
proliferation;
NF-κB
Erscheinungsjahr
2023
Zeitschriftentitel
Cells
Band
12
Ausgabe
23
Art.-Nr.
2683
Urheberrecht / Lizenzen
eISSN
2073-4409
Page URI
https://pub.uni-bielefeld.de/record/2984752
Zitieren
Niemann T, Joneleit J, Storm J, et al. Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells. Cells. 2023;12(23): 2683.
Niemann, T., Joneleit, J., Storm, J., Nacke, T., Wähnert, D., Kaltschmidt, C., Vordemvenne, T., et al. (2023). Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells. Cells, 12(23), 2683. https://doi.org/10.3390/cells12232683
Niemann, Tarek, Joneleit, Jonas, Storm, Jonathan, Nacke, Tom, Wähnert, Dirk, Kaltschmidt, Christian, Vordemvenne, Thomas, and Kaltschmidt, Barbara. 2023. “Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells”. Cells 12 (23): 2683.
Niemann, T., Joneleit, J., Storm, J., Nacke, T., Wähnert, D., Kaltschmidt, C., Vordemvenne, T., and Kaltschmidt, B. (2023). Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells. Cells 12:2683.
Niemann, T., et al., 2023. Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells. Cells, 12(23): 2683.
T. Niemann, et al., “Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells”, Cells, vol. 12, 2023, : 2683.
Niemann, T., Joneleit, J., Storm, J., Nacke, T., Wähnert, D., Kaltschmidt, C., Vordemvenne, T., Kaltschmidt, B.: Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells. Cells. 12, : 2683 (2023).
Niemann, Tarek, Joneleit, Jonas, Storm, Jonathan, Nacke, Tom, Wähnert, Dirk, Kaltschmidt, Christian, Vordemvenne, Thomas, and Kaltschmidt, Barbara. “Analyzing Sex-Specific Dimorphism in Human Skeletal Stem Cells”. Cells 12.23 (2023): 2683.
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Daten bereitgestellt von European Bioinformatics Institute (EBI)
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Daten bereitgestellt von Europe PubMed Central.
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Material in PUB:
Dissertation, die diesen PUB Eintrag enthält
Sexual dimorphism of adult human stem cells during neuronal & osteogenic differentiation
Niemann T (2024)
Bielefeld: Universität Bielefeld.
Niemann T (2024)
Bielefeld: Universität Bielefeld.
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